Research Article Influence of Thickness on the Holographic Parameters of H-PDLC Materials

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1 International Polymer Science, Article ID , 7 pages Research Article Influence of Thickness on the Holographic Parameters of H-PDLC Materials S. Gallego, 1,2 M. Ortuño, 1,2 A. Márquez, 1,2 R. Fernández, 1 M. L. Álvarez, 1,2 A. Beléndez, 1,2 and I. Pascual 1,3 1 Instituto Universitario de Física Aplicada a las Ciencias y las Tecnologías, Universidad de Alicante, Apartado 99, 38 Alicante, Spain 2 Departamento de Física, Ingeniería de Sistemas y Teoría de la Señal,UniversidaddeAlicante,Apartado99,38Alicante,Spain 3 Departamento de Óptica, Farmacología y Anatomía, Universidad de Alicante, Apartado 99, 38 Alicante, Spain Correspondence should be addressed to S. Gallego; sergi.gallego@ua.es Received 15 July 214; Accepted 5 November 214; Published 15 December 214 Academic Editor: Michael R. Gleeson Copyright 214 S. Gallego et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For photopolymers the compound concentrations and final thickness of the sample should be known in order to model hologram formation and introduce the reaction-diffusion kinetics of the monomer-polymer system. In principle the cell thickness can be controlled by bead spacers between the two pieces of ITO glass. In this paper we report a study of the influence of thickness on the holographic properties of this type of materials. To fit the physical and optical thickness of the samples we used the rigorous coupled wave analysis assuming an exponential decay in the refractive index modulation. 1. Introduction Photopolymers are one of the most promising holographic recording media for many technological applications, from integrated optical waveguide fabrication to optical data storage [1 5]. Their versatility is well known and new possibilities were created by including new components, such as nanoparticles or dispersed liquid crystal molecules in classical formulations, making them interesting for additional applications [6 8]. For example, the ability to control the diffraction efficiency of holographic optical elements by applying an electric field leads to the possibility of using HOEs in dynamic applications for agile beam steering, nonlinear optics, and optical switching devices [9]. Holographic polymer dispersed liquid crystals are known as H-PDLCs. They are made by holographic recording in a photopolymerization induced phase separation process (PIPS) in which the liquid crystal molecules diffuse to dark zones in the diffraction grating where they can be oriented by means of an electric field. The orientation of the liquid crystal produces a refractive index variation which changes the diffraction efficiency. Therefore, the grating develops a dynamic behavior that may be modified by electronic means. In this manner, it is possible to make dynamic devices such as tunable-focus lenses, sensors, phase modulators, or prism gratings [1 16]. There are many parameters involved in hologram formation. This process comprises a number of mechanisms, including photoinitiation, polymerization, diffusion, LC phase separation, and shrinkage. Several models have been developed for the formation of holograms in photopolymers [17 25]. The most recent models incorporate an initiation process, the peculiar properties of phase-separated LCs, development of anisotropic gratings, size of the polymer chains and scattering, and so forth [26]. As opposed to dry photopolymers where the quantity of solvent used up during the drying process must be measured in order to calculate the final component concentrations [27], in HPDLCs, it can be assumed in principle that the concentration of each component remains constant once it is deposited between two glass plates. These parameters are important in order to simulate the material behavior correctly during recording. Alternatively, using experimental performance optimization other parameters have been analyzed [28]. In this sense many researchers have explored different material recipes to achieve high diffraction efficiency [28], fast response time,

2 2 International Polymer Science low drive voltage, and so forth. Some of the effects analyzed are exposure intensity, exposure temperature, monomer functionality, LC concentration, NVP concentration, driving voltage, surfactant, fluorination, index matching, and nanoparticle doping [29]. Nevertheless, the effect of the thickness of the sample on grating morphology has not yet been studied in depth. Usually the prepolymer syrup is prepared under dark conditions (or visible light at a wavelength where the dye does not absorb) and then sandwiched between two conductive ITO glass plates separated using glass microspheres. In order to obtain samples of the same physical thickness, a weight of 1 kg was placed over the layer for 5 minutes. As a result we obtained a probabilistic physical thickness distribution with values higher than the diameter of the microspheres used between the ITO glasses. Usually the HPDLC plates are thinner than 4 μm in order to achieve the reorientation of the liquid crystal molecules applying an electric field not so big. The goal of this paper is to analyze the effect of this thickness variation on the holographic behavior of some chemical compositions of HPDLC materials. In particular the final thickness of the samples is directly related to the dye concentrationrequiredtoobtainenoughlightabsorptionand energetic sensitivity without large attenuation in depth of the refractive index profile [3]. In this sense we analyzed the effect of dye concentration on the properties of the transmission diffraction gratings recorded. In order to achieve a deeper insight into this aspect, we analyzed the evolution of diffraction efficiency as a function of exposure and used the fitting of the angular response of the hologram around the first Bragg angle to calculate the physical and optical thickness [3] and attenuation of refractive index modulation in depth. We used an algorithm based on the rigorous coupled wave theory [31] where an exponential decay in the refractive index modulation, Δn, is assumed [32] andα n is the coefficient of the depth attenuation refractive index modulation. In order to apply the RCW to obtain the efficiency of the different orders we studied a periodic structure: the hologram was divided into G different subgratings of thickness d g each. The total thickness of the hologram, d, can be obtained from the sumofthethicknessesofthedifferentsubgratings: d= G g=1 d g, (1) where G is the number of gratings retained. Each subgrating is assumed to have a periodic dielectric permittivity of the form ε g (x) = ε g,h exp [jhkx], (2) h where K is the modulus of the grating vector and ε g,h is the hth Fourier component of the relative permittivity in the grating sublayer g,whichcanbeexpressedas ε g,h =ε,h exp [ α n [ g g =1 d g ]. (3) ] It is important to use for H-PDLC gratings a rigorous wave analysis for many reasons. One of them is the proximity of the border between thick and thin holograms because of the small values of thickness analyzed between 13 and 37 μm and the high values of the refractive index modulation stored between.5 and.36. In addition it is important to note that along this work we mention the index modulation, Δn, which is the index modulation at the beginning of the grating, since the depth attenuation on the last part of the material is clearly smaller. Finally we want to remark that for the reading beam used in this work our material is 1% transparent; nevertheless part of the energy is reflected due to the Fresnel losses for TE polarization; in addition due to the scattering thefinaldemeasuredwillbereduced.thisscatteredenergy depends on the coefficient of attenuation and scattering, α s, as follows: DE =e α sd/ cos θ DE, (4) where d is the physical thickness of the layer and θ is the angle of the beam with respect to the normal inside the hologram. 2. Experimental Setup The monomer used was dipentaerythritol penta-/hexaacrylate (DPHPA) with a refractive index n = 1.49.Weused the nematic liquid crystal, Licristal BL36 from Merck. It is a mixture of 4-cyanobiphenyls with alkyl chains of different lengths. It has an ordinary refractive index n = and a difference between extraordinary and ordinary index Δn =.267 [28]. There is a difference of.37 between the ordinary refractive index of the liquid crystal and that of the monomer. The liquid crystal concentration was set at 28 wt% as the starting point for component optimization and remained practically unchanged during this process. N-vinyl-2-pyrrolidone was used as crosslinker, N-phenylglicine (NPG) as radical generator, octanoic acid (OA) as cosolvent [28], and ethyl eosin (YEt) as dye. N-methyl-2- pyrrolidone was used in combination with NVP in order to control overmodulation during hologram recording. The prepolymer solution was made by mixing the components under red light where the material is not sensitive. The solution was sonicated in an ultrasonic bath, deposited between two conductive ITO glass plates 1 mm thick and separated using two types of glass microspheres. The first type of microspheres was provided by Aldrich with a thickness between 9 and 13 μm and the second type was provided by Whitehouse Scientific with a thickness between 2 and 3 μm. The device was exposed to a laser beam (λ = 532 nm) in a holographic setup in order to record a diffraction grating in the photopolymer layer. A photopolymerization reaction takes place in the bright zones of the diffraction grating and a highly reticulated polymer network is generated. The liquid crystal molecules diffuse to the unexposed region where they remain as droplets. In this work we used three different chemical compositions and the refractive indexes of the final mixture are represented in Table 1.In the first two chemical compositions we analyzed the influence of

3 International Polymer Science 3 Table 1: Composition of photopolymers 1, 2, and 3 in wt% and the refractive index of the final mixture. Photopolymer DPHPA BL36 YEt NPG NVP OA NMP n M1 M2 O1 Sample holder O2 Motion control PC Nd: YAG laser (532 nm) θ θ D3 M7 M8 L3 SF3 BS L1 D1 D2 L2 SF2 M3 M5 M6 SF1 M4 He-Ne laser (633 nm) Figure 1: Experimental setup. BS: beamsplitter, Mi: mirror, SFi: spatial filter, Li: lens, Di: diaphragm, Oi: optical power meter, and PC: data recorder. Number of samples Thickness (μm) Figure 2: Number of samples as a function of the physical thickness using chemical composition 1 and microspheres 13 μmindiameter, hollow squares. Gaussian distribution, solid line. 3. Results and Discussion the dye concentration on the optical thickness of the diffraction gratings. In the case of composition 3, the analysis described in [28] was done to control overmodulation and obtain stable maximum diffraction efficiency. We monitored the diffraction grating in real time using red light (λ = 633 nm) where the dye does not absorb. After recording, when the green laser was shut off, we rotated the sample to record the angular response around the Bragg angle and obtained the data necessary to calculate the physical and optical thickness of the holographic diffraction gratings. The experimental device is shown in Figure 1.AnNd:YAG laser tuned at a wavelength of 532 nm was used to record diffraction gratings by means of continuous laser exposure. The laser beam was split into two secondary beams with an intensity ratio of 1 : 1. The diameter of these beams was increased to 1 cm using a spatial filter and collimating lens, while spatial filtering was ensured. The object and reference beams were recombined at the sample at an angle of 16 degrees to the normal with an appropriate set of mirrors, and the spatial frequency obtained was 136 lines/mm. The working intensity at 532 nm was 7 mw/cm 2, and the exposure time was 6 s. The diffracted and transmitted intensity were monitored in real time with a He-Ne laser positioned at Bragg s angle (19.1 ) tuned to 633 nm, where the material does not polymerize. The diffraction efficiency was calculated as the ratio of the diffracted beam (I D ) to the incident power (I ). In this section we present the results obtained after recording hundreds of diffraction gratings between 13 and 4 μm. As we explained in the introduction, the physical thicknesses of the samples are always greater than the diameter of the microspheres. The values obtained using the 13 μm thick Aldrich microspheres and chemical composition 1 for 135 samples are shown in Figure 2. Wecanestimatetheerror in calculating the thickness, using the method described in the introduction section, at less than 1 μm. We can see that a high probability occurs between 2 and 21 μm. In addition 7% of the samples have a thickness between 17 and 25 μm. Comparing these results, with a Gaussian distribution with a mean or expectation equal to 2.5 and standard deviation equal to 3.5, to the experimental data, we can verify a similar behavior. Figure 3 shows one angular response fitted using the algorithm based on RCW taking into account the exponential decay of the refractive index modulation. In particular Figure 3 corresponds to the 29 μm thickgrating with a refractive index modulation of.15, an attenuation coefficient for the refractive index modulation, α n,of.3 μm 1, and a coefficient of attenuation and scattering, α s, of.5 μm 1. Analyzing this figure the clear effects of the overmodulation of the refractive index can be detected. This figure shows good agreement between the experimental data andthesimulationprovidedbythealgorithm[32] aswellas a smoothing of the secondary lobes due to the attenuation in depth of the refractive index that justify the use of

4 4 International Polymer Science Diffraction efficiency Angle (deg.) Figure 3: Diffraction efficiency as a function of the readout angle for agrating 29μm thick, hollow circles, and the fitting provided by the algorithm using composition 1. the algorithm to fit the angular scan and measure the physical and optical thickness Effect of Dye Concentration. Ethyl eosin, the dye, is bleached like the typical xanthene dyes during the photoinitiation process [28]. Bearing this in mind, a high dye concentration is required for applications like multiplexing data pages, where the thickness of the samples is greater than 25μm. However, a high concentration of dye increases scattering and damages the morphology of the recorded holograms [33]. Furthermore, increasing the dye concentration can modify the optical thickness of the diffraction grating or the attenuation of the refractive index modulation in depth [3]. As opposed to photopolymer holographic memories, H- PDLC materials contain mainly polyfunctional monomers in order to achieve an effective PIPS effect. Polyfunctional monomers give rise to a high degree of reticulation of the polymer chains in a short time and therefore high refractive index modulation at a lower exposure than do standard photopolymers without liquid crystals. For this reason, the dye content in H-PDLC materials, where very thin layers are required, must be very small. In the literature the concentration of the dye YEt changes in the range of.7% normally used when a dye is optimized in standard photopolymers [28]. In this work we used two compositions, 1 and 2, that had given us good results in previous studies. In order to avoid an undesired increase in scattering with composition 2, we used the microspheres provided by Whitehouse Scientific to increase the physical thickness slightly. The diffraction efficiency during 4 s of exposure for different ranges of thicknesses is shown in Figure 4: Figure 4(a) for composition 1 and Figure 4(b) for composition 2. As can be seen for composition 1 the maximum DE is achieved with an exposure of around 9 mj/cm 2 and for composition 2 of around 7 mj/cm 2. Taking into account results for not coverplated photopolymers [34],where anincreaseinthickness produces an important increase in the energetic sensitivity of the material, important changes can be expected in the holographic behavior of the HPDLC layers. However, from an initial analysis of the two figures it is hard to clarify the specific influence of thickness on diffraction efficiency during recording. The diffraction behavior looks very similar. At best we can say that the gratings with low values of thickness exhibit slightly better energetic sensitivity. It is important to note that we defined this parameter as the exposure required toachievethemaximumvalueofde,orinotherwordshow fast is the increase of the DE as a function of time after the inhibition period. In other words, they achieve maximum DE faster than the thicker ones. All the gratings have the same spatial frequency; therefore, we know that the diffraction efficiency depends on the product of optical thickness and refractiveindex modulation [35]. If these layers have different thicknesses, obviously they have different refractive index modulations. In order to delve deeper into this phenomenon and obtain quantitative information about the refractive index modulation, we fitted the angular responses of different gratings just a few seconds after exposure. In Figure 5 we present the results for both, composition 1 and composition 2, the inverse of the average refractive index modulation as a function of the thickness. The linearity in this behavior, for bothcases,meansthattheproductofthicknessandrefractive index modulation remains almost constant. These values were measured after 6 s of exposure, when the gratings are in the saturation zone and the polymerization has finished for a range of thickness between 13 and 37 μm. The results obtained for composition 2 are similar. We will compare directly the two dye concentrations at the end of this section using the data fitted from the angular response. The data presented in Figure 5 suggest that the concentration of components in the sample decreases with increasing thickness. We measure the area of the polymer layer for each sample and it is always around 4 cm 2. Using the proposed algorithm to analyze the angular response around Bragg s angle we also obtain the values of α s and α n. As can be expected the average of these values decreases with thickness. For composition 1 the thinnest layers present values of α n up to.9 μm 1 and of α s up to.6 μm 1, whereas the values of both these parameters for thicker layers (over 3 μm) are around.3 μm 1. Tocompleteourstudyoftheinfluenceofthedyeconcentration, it is necessary to compare chemical compositions 1 and 2 using the same range of thicknesses. The results (average values) are presented in Table 2. Fromacomparison of the two chemical compositions it may be seen that if the dye concentration is doubled, the refractive index increases; however, there is also an undesirable increase in parameters such as α s and α n.ahighvalueofα s implies a lower quality in the recorded hologram and the DE; on the other hand, α n only affects the optical thickness and the angular selectivity around Bragg s angle; thus α n is less critical than α s. Letuspresentthedirectcomparisonduringrecording for compositions 1 and 2. In Figure 6 we can see the obvious

5 International Polymer Science Diffraction efficiency (%) Diffraction efficiency (%) E (mj/cm 2 ) E (mj/cm 2 ) 2 μm 16 μm 19 μm 14 μm 18 μm 37 μm 23 μm 28 μm 31 μm 33 μm (a) (b) Figure 4: (a) Diffraction efficiency as a function of recording exposure; sample thickness between 14 and 2 μm using composition 1.(b) Diffraction efficiency as a function of recording exposure; sample thickness between 23 and 37 μm using composition R 2 =.9933 Table 2: Main parameters fitted from the angular response for chemical compositions 1 and 2 after recording. Chemical composition Thickness (μm) Refractive index modulation α n (μm 1 ) α s (μm 1 ) /Δn 6 4 R 2 = Physical thickness (μm) Composition 1 Composition 2 Figure 5: The inverse of the refractive index modulation as a function of physical thickness for the layers with chemical composition 1. different behavior of these compounds under sinusoidal illumination; nevertheless the final DE is very similar: 5% for composition 1 and 4% for composition 2. After fitting of the angular response we can determine that both samples havethesamephysicalthickness(3 ± 1) μm; however, the material with higher dye concentration presents better energetic sensitivity and higher value of refractive index modulation; the DE after 1 s of exposure is low due to the overmodulation effects. It is important to note that the maximum of DE is smaller, 77% versus 82% for composition 1, due to the larger value of α s, scattering coefficient. In this sense,itisimportanttoremarkthatthepresenteddataarenot corrected to take into account the Fresnel losses. Taking into account the maximum DE, TE polarization is around 86% Layers without Overmodulation. As we have shown in a previous paper, incorporation of 3% NMP in the H-PDLC formulation leads to an improved result in order to obtain higher values of diffraction efficiency after saturation [28]. The diffraction efficiency curve is stabilized with a high value of DE preventing overmodulation during hologram recording. This makes it possible to obtain a high DE max at the end of the exposure and therefore a better performance in photopolymers with ethyl eosin as dye. In this section we present the same study for composition 3. Figure 7 shows diffraction efficiency as a function of exposure for four different thicknesses. In this case after saturation the diffraction efficiency remains close to the maximum due to the presence of NMP. As, in the case of Figure 4,thefourdifferent thicknesses present very similar behaviors and energetic sensitivity. We followed the same steps to calculate the data in Table 3 and from this table we can extract similar results.

6 6 International Polymer Science Diffraction efficiency (%) E (mj/cm 2 ) Composition 1 Composition 2 Table 3: Main parameters fitted from the angular response for chemical composition 3. Thickness (μm) Refractive index modulation α n (μm 1 ) α s (μm 1 ) of the hologram and scattering. Therefore, we underline the importance of controlling the thickness of H-PDLC materials in order to achieve high values of reproducibility in all the holographic parameters not only in diffraction efficiency. Figure 6: Comparison between the recording processes for compositions1 and 2for layers 3μm thick. Diffraction efficiency (%) E (mj/cm 2 ) 25 μm 27 μm 3 μm 37 μm Figure 7: Diffraction efficiency as a function of recording exposure; sample thickness between 25 and 37 μmusingcomposition3. An increase in thickness implies a low concentration of the component in the syrup due to the capillarity action of the prepolymer syrup and the associate adhesive forces between the liquid and ITO glass substrate; thus the refractive index modulation decreases more or less linearly, and parameters such as α s and α n decrease too. 4. Conclusions We analyzed the effects of thickness on the final holographic properties of H-PDLC materials with different chemical compositions. We demonstrated that the product of refractive index modulation and thickness (diffraction efficiency) remains constant for layers with the same chemical composition over a wide range of thicknesses due to the inverse, linear variation of these two parameters. In addition we showed that an increase in dye concentration affects the depth attenuation Conflict of Interests The authors declare that there is no conflict of interests regarding the publication of this paper. Acknowledgments The work was supported by the Ministerio de Economía y Competitividad of Spain under Projects FIS C2-1 and FIS C2-2 and by the Generalitat Valenciana of Spain under Projects PROMETEO/211/21 and ISIC/212/13. References [1] J. Neumann, K. S. Wieking, and D. Kip, Direct laser writing of surface reliefs in dry, self-developing photopolymer films, Applied Optics, vol. 38, no. 25, pp , [2] X. T. Li, A. Natansohn, and P. Rochon, Photoinduced liquid crystal alignment based on a surface relief grating in an assembled cell, Applied Physics Letters,vol.74,no.25,pp , [3] A. Márquez,S.Gallego,M.Ortuño et al., Generation of diffractive optical elements onto a photopolymer using a liquid crystal display, in Optical Modelling and Design, vol of Proceedings of SPIE,May21. [4] M. D. Lechner, Photopolymers for optical memories and waveguides, in Electronic Properties of Polymers and Related Compounds,vol.63ofSpringer Series in Solid-State Sciences,pp.31 38,Springer,NewYork,NY,USA,1985. [5] H.J.Coufal,D.Psaltis,andG.T.Sincerbox,Eds.,Holographic Data Storage, Springer, Berlin, Germany, 2. [6] N. Suzuki and Y. Tomita, Silica-nanoparticle-dispersed methacrylate photopolymers with net diffraction efficiency near 1%, Applied Optics,vol.43,no.1,pp ,24. [7] E. Hata, K. Mitsube, K. Momose, and Y. Tomita, Holographic nanoparticle-polymer composites based on step-growth thiolene photopolymerization, Optical Materials Express,vol.1,no. 2, pp , 211. [8] M. A. Ellabban, I. Drevenšek-Olenik, and R. A. Rupp, Huge retardation of grating formation in holographic polymerdispersed liquid crystals, AppliedPhysicsB:LasersandOptics, vol.91,no.1,pp.11 15,28.

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